Effects of Ginkgo biloba extract on SOD, GSH-Px and MDA in brain tissue of rats during cerebral ischemia and reperfusion
Li Shen, Fang Guo, Junxia Li, Shen Fu, Song Gao
Abstract
Li Shen, Fang Guo, Junxia Li, Shen Fu, Song Gao
Abstract
AIM: To observe the effects of Ginkgo biloba extract (GbE)solution on SOD, GSH-Px and MDA in cortex of rats during cerebral ischemia and reperfusion. METHODS: Seventy-eight Sprague-Dawley (SD) rats were divided randomly into thirteen groups: sham control group, intraperitoneal injection of saline; ischemia-reperfusion groups, including ischemia (I) with 2 h/reperfusion(R) 1, 2, 3 h groups, injected intraperitoneally(ip) saline before reperfusion 1 h, respectively; Gb E A treatment groups, including I 2 h/R 1, 2, 3 h groups, ip Gb E A 5 mg·kg -1 before reperfusion 1 h, respectively; GbE B 5,10 mg·kg -1 treatment groups, including I 2 h/R 1,2,3 h groups, ip GbE B 5,10 mg·kg -1 before reperfusion 1 h, respectively. The model of focal cerebral ischemia-reperfusion was established with ligation of rat middle cerebral artery. Xanthine oxidase, DTNB and TBA were utilized for detecting activities of SOD, GSH-Px and contents of MDA in brain tissue, respectively. RESULTS: Comparing determining the ischemia-reperfusion control to treatment groups, GbE B injection can dose-dependently increase the activities of SOD and GSH-Px(P0.05) and decrease contents of MDA(P 0.05). There was no significant difference between GbE B 5 mg·kg -1 groups and GbE A 5 mg·kg -1 groups(P0.05). CONCLUSION: GbE B injection could protect brain from ischemia-reperfusion injury with increase vitality to resist oxidation of brain tissue and decrease content of MDA.
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AIM: To observe the effects of Ginkgo biloba extract (GbE)solution on SOD, GSH-Px and MDA in cortex of rats during cerebral ischemia and reperfusion. METHODS: Seventy-eight Sprague-Dawley (SD) rats were divided randomly into thirteen groups: sham control group, intraperitoneal injection of saline; ischemia-reperfusion groups, including ischemia (I) with 2 h/reperfusion(R) 1, 2, 3 h groups, injected intraperitoneally(ip) saline before reperfusion 1 h, respectively; Gb E A treatment groups, including I 2 h/R 1, 2, 3 h groups, ip Gb E A 5 mg·kg -1 before reperfusion 1 h, respectively; GbE B 5,10 mg·kg -1 treatment groups, including I 2 h/R 1,2,3 h groups, ip GbE B 5,10 mg·kg -1 before reperfusion 1 h, respectively. The model of focal cerebral ischemia-reperfusion was established with ligation of rat middle cerebral artery. Xanthine oxidase, DTNB and TBA were utilized for detecting activities of SOD, GSH-Px and contents of MDA in brain tissue, respectively. RESULTS: Comparing determining the ischemia-reperfusion control to treatment groups, GbE B injection can dose-dependently increase the activities of SOD and GSH-Px(P0.05) and decrease contents of MDA(P 0.05). There was no significant difference between GbE B 5 mg·kg -1 groups and GbE A 5 mg·kg -1 groups(P0.05). CONCLUSION: GbE B injection could protect brain from ischemia-reperfusion injury with increase vitality to resist oxidation of brain tissue and decrease content of MDA.
Key concepts: Ginkgo biloba, Ischemia, Xanthine oxidase, Intraperitoneal injection, Pharmacology, Saline, Reperfusion injury, Neuroprotection